Tag Archives: Public Health and Medical Professionals for Transparency

Somehow The Mainstream Media Missed This Story

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On Friday, The Epoch Times reported the following:

Pfizer hired 600 employees in the months after its COVID-19 vaccine was authorized in the United States due to the “large increase” of reports of side effects linked to the vaccine, according to a document prepared by the company.

Pfizer has “taken a multiple actions to help alleviate the large increase of adverse event reports,” according to the document. “This includes significant technology enhancements, and process and workflow solutions, as well as increasing the number of data entry and case processing colleagues.”

At the time when the document—from the first quarter of 2021—was sent to the U.S. Food and Drug Administration (FDA), Pfizer had onboarded about 600 extra full-time workers to deal with the jump.

“More are joining each month with an expected total of more than 1,800 additional resources by the end of June 2021,” Pfizer said.

The document was titled a “cumulative analysis of post-authorization adverse event reports” of Pfizer’s vaccine received through Feb. 28, 2021. It was approved by the FDA on April 30, 2021.

The document was not made public until the Public Health and Medical Professionals for Transparency sued the FDA after the agency claimed it needed decades to produce all the documents relating to the emergency use authorization granted to the company for the vaccine.

Under an agreement reached in February, the FDA must produce a certain number of pages each month.

The article concludes:

Pfizer did not respond to emailed questions, including how many workers it has onboarded to deal with adverse events.

The companies that manufacture the other two COVID-19 vaccines that U.S. regulators have cleared, Moderna and Johnson & Johnson, did not respond when asked if they have seen an increase in adverse events and if they have hired more employees to deal with reports.

The number of post-vaccination adverse event reports to the Vaccine Adverse Event Reporting System, jointly run by the FDA and the Centers for Disease Control and Prevention, has spiked since the vaccines were first cleared.

Problems linked to the vaccines include heart inflammation, blood clotting, and severe allergic shock.

Federal officials say the vaccines’ benefits outweigh the risks, but some experts are increasingly questioning that assertion, particularly for certain populations.

People should have been made aware of this as the vaccine was being pushed by the government. A vaccine that doesn’t prevent the illness and has serious side effects does not seem to be the answer to the pandemic. Please follow the link above to read the entire article. If you are not yet vaxxed, you might not want to rush out to receive the vaccination.

The Facts Are Slowing Coming Out

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On Thursday, The Patriot Daily Wire reported that the Food and Drug Administration (FDA) has released more information about the possible side effects of the Pfizer coronavirus vaccine.

The article reports:

As the FDA prepares to approve Pfizer’s new pill for treating high-risk patients infected with COVID, more information about dangerous side effects tied to its vaccine are coming to light.

Just yesterday, we reported another death tied to the vaccine in New Zealand. Now, documents released by the FDA reveal that drugmaker Pfizer recorded nearly 160K adverse reactions to its COVID vaccine in the initial months of its rollout.

The data were obtained by a group of doctors, professors, and journalists calling themselves Public Health and Medical Professionals for Transparency. They filed a Freedom of Information Act request with the FDA asking for their release. And the first tranche of documents revealed that, as of February 2021, when Pfizer’s shot was being rolled out worldwide on an emergency basis, the drugmaker had compiled more than 42K case reports detailing nearly 160K individual adverse reactions to the vaccine.

The data show the bulk of the adverse event cases, both serious and non-serious, were classified as “general disorders”.

You shouldn’t have to file a Freedom of Information request to get this data–it should be given to everyone who is considering getting the vaccine.

Please follow the link above to read the entire article. It includes the complete breakdown of data from Public Health and Medical Professionals For Transparency. There has to be a risk/benefit analysis when considering getting the vaccine. There also needs to be a discussion about how effective the vaccine actually is.

The Search For Transparency

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On Wednesday, NewsMax posted an article about the Food and Drug Administration’s (FDA) timeline in releasing data on the Pfizer vaccine.  The FDA has requested 75 years to produce the data.

The article reports:

Public Health and Medical Professionals for Transparency has filed Freedom of Information Act requests for the data, which the FDA at first said would take 55 years to produce at 500 pages per month for the entire 329,000 page cache of documents.

Now the FDA is asking a judge to give it 75 years to produce the data, saying there’s over 59,000 more pages than weren’t mentioned in the first request. That would take the full release to 2096, wrote Aaron Siri, a lawyer working on the case.

“If you find what you are reading difficult to believe — that is because it is dystopian for the government to give Pfizer billions, mandate Americans to take its product, prohibit Americans from suing for harms, but yet refuse to let Americans see the data underlying its licensure,” he wrote.

The medical group is suing to speed things up.

The group says the data should be made public quickly because the FDA spent only 108 days reviewing it before granting emergency use authorization to the Pfizer-BioNTech vaccine — and because vaccine mandates are being issued by local and federal entities, Epoch Times reported.

The article concludes:

On Dec. 2, Rep. Ralph Norman, R-S.C., introduced a bill calling for the head of the FDA to release all records about the vaccine in 100 days.

“Since the Biden administration is hell-bent on forcing these vaccine mandates on us, the public has every right to know how this vaccine was approved, especially in such a short amount of time,” he said in a statement. “After all, the FDA managed to consider all 329,000 pages of data and grant emergency approval of the Pfizer vaccine within just 108 days.”

The article cites what I think is one of the most important issues here:

that is because it is dystopian for the government to give Pfizer billions, mandate Americans to take its product, prohibit Americans from suing for harms, but yet refuse to let Americans see the data underlying its licensure

That should not happen in a free country.